"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SPTB"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 807128	NM_001355436.2(SPTB):c.6351AGA[1] (p.Glu2119del)	SPTB (E2119del)	Microsatellite (inframe_deletion)	Elliptocytosis 3 +2 more	GUncertain significance
Select item 994361	NM_001355436.2(SPTB):c.4474-17C>T	SPTB	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1679426	NM_001355436.2(SPTB):c.3764+9G>A	SPTB	Single nucleotide variant (intron variant)	Elliptocytosis 3 +2 more	GBenign/Likely benign

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